Quality Engineer, Product Development Specialist

1 week ago


Sturgis, Michigan, United States Abbott Laboratories Full time

About Abbott Laboratories

Abbott Laboratories is a global leader in healthcare, dedicated to helping people live more fully at all stages of life. Our diverse portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals, and pharmaceuticals.

We serve over 160 countries, employing 114,000 colleagues worldwide. At Abbott, you can do meaningful work, grow professionally, care for yourself and your family, be your authentic self, and enjoy a full life.

Benefits and Rewards

  • Competitive salary: $74,100 - $144,400 per year
  • A comprehensive benefits package, including medical, dental, vision, wellness programs, and retirement plans
  • 120 hours of accrued vacation, plus vacation buy program and 10 paid holidays
  • Tuition reimbursement and education benefits
  • A stable company with strong financial performance and commitment to community involvement

The Opportunity

This Quality Engineer position is based in Sturgis, MI, within the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from infants to adults.

You will work on developing and maintaining quality engineering methodologies and providing quality support in new product development, manufacturing, or system/services support.

Responsibilities

  • Identify and implement process control systems to meet or exceed internal and external requirements
  • Lead and coach non-exempt and exempt personnel
  • Develop and execute streamlined business systems to resolve quality issues
  • Apply systematic problem-solving methodologies to identify and communicate quality issues
  • Design and conduct experiments for process optimization and improvement

Requirements

  • Bachelor's degree in a relevant field, plus 2-5 years of experience, or a Master's degree with 1-3 years of experience
  • Demonstrated use of quality tools and methodologies, with detailed knowledge of FDA and GMP regulations
  • Strong project management and leadership skills, with advanced computer skills and statistical analysis abilities


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